Variant report

Variant	rs28687057
Chromosome Location	chr4:120280812-120280813
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10002914	0.81[AMR][1000 genomes]
rs10021601	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10029303	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10434028	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10517834	0.81[AMR][1000 genomes]
rs10857066	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11098505	0.81[AMR][1000 genomes]
rs11098507	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12374244	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12374245	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12374352	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12374396	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12499602	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12503082	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12510487	0.81[AMR][1000 genomes]
rs13104572	0.82[AMR][1000 genomes]
rs13105020	0.81[AMR][1000 genomes]
rs13132082	0.81[AMR][1000 genomes]
rs28470894	0.84[AMR][1000 genomes]
rs28488261	0.84[AMR][1000 genomes]
rs28501434	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28581362	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28594160	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28668103	0.81[AMR][1000 genomes]
rs60378962	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs67281037	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6824111	0.81[AMR][1000 genomes]
rs6824169	0.81[AMR][1000 genomes]
rs6846966	0.82[AMR][1000 genomes]
rs6847586	0.81[AMR][1000 genomes]
rs6847778	0.81[AMR][1000 genomes]
rs6847862	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6848081	0.83[AMR][1000 genomes]
rs6848380	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6857892	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7677068	0.81[AMR][1000 genomes]
rs9991221	0.81[AMR][1000 genomes]
rs9995136	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv879841	chr4:120244085-120388406	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv879842	chr4:120244085-120424087	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv427694	chr4:120250511-120501728	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	esv2538163	chr4:120252854-120388678	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv964091	chr4:120255342-120290951	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs28687057	LOC645513	Cis_1M	lymphoblastoid	RTeQTL
rs28687057	FLJ14186///LOC284701///LOC441124///LOC728624	Cis_1M	lymphoblastoid	RTeQTL
rs28687057	RP11-33B1.1	cis	Nerve Tibial	GTEx
rs28687057	RP11-33B1.4	cis	Whole Blood	GTEx
rs28687057	RP11-33B1.1	cis	Whole Blood	GTEx
rs28687057	RP11-384K6.6	cis	Whole Blood	GTEx
rs28687057	RP11-33B1.1	cis	Heart Left Ventricle	GTEx
rs28687057	RP11-33B1.1	cis	lung	GTEx
rs28687057	RP11-33B1.1	cis	Esophagus Mucosa	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120269600-120293000	Weak transcription	Fetal Heart	heart
2	chr4:120280800-120282000	Enhancers	HepG2	liver

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